QUALITY CONTROL RESEARCH ASSOCIATE
IN SANTA MONICA, CA, USA!
Date Posted: 08/14/2025
Hiring Organization: Rose International
Position Number: 487045
Industry: Biotech/Healthcare
Job Title: Quality Control Research Associate
Job Location: Santa Monica, CA, USA, 90404
Work Model: Onsite
Shift: 8 - 5 PT
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 6
Min Hourly Rate($): 30.00
Max Hourly Rate($): 37.00
Must Have Skills/Attributes: Analysis, Manufacturing, MS Office
Experience Desired: Experience conducting quality Control Analytical testing (2 yrs); Perform reviews of assays and maintain the laboratory in a state of compliance (2 yrs)
Required Minimum Education: Bachelor's Degree
Preferred Education: Master's Degree
**C2C is not available**
Job Description
Top Required Skills:
Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment
Perform reviews of assays and maintain the laboratory in a state of compliance
Responsibilities:
Conduct non-routine analysis of raw materials, intermediates, and finished product samples
Write and execute protocols and reports
Evaluate purchase equipment and perform installations and qualifications of new instruments
Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment
Perform reviews of assays and maintain the laboratory in a state of compliance
Troubleshoot instrumentation and test methods
Assist in the training of QC staff as needed
Apply knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices
Demonstrate working knowledge and proficiency with Microsoft Office software
Write and execute protocols and SOPs
**Only those lawfully authorized to work in the designated country associated with the position will be considered.**
**Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit . Should you have any questions/concerns, via our secure .
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' .
IN SANTA MONICA, CA, USA!
Date Posted: 08/14/2025
Hiring Organization: Rose International
Position Number: 487045
Industry: Biotech/Healthcare
Job Title: Quality Control Research Associate
Job Location: Santa Monica, CA, USA, 90404
Work Model: Onsite
Shift: 8 - 5 PT
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 6
Min Hourly Rate($): 30.00
Max Hourly Rate($): 37.00
Must Have Skills/Attributes: Analysis, Manufacturing, MS Office
Experience Desired: Experience conducting quality Control Analytical testing (2 yrs); Perform reviews of assays and maintain the laboratory in a state of compliance (2 yrs)
Required Minimum Education: Bachelor's Degree
Preferred Education: Master's Degree
**C2C is not available**
Job Description
Top Required Skills:
Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment
Perform reviews of assays and maintain the laboratory in a state of compliance
Responsibilities:
Conduct non-routine analysis of raw materials, intermediates, and finished product samples
Write and execute protocols and reports
Evaluate purchase equipment and perform installations and qualifications of new instruments
Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment
Perform reviews of assays and maintain the laboratory in a state of compliance
Troubleshoot instrumentation and test methods
Assist in the training of QC staff as needed
Apply knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices
Demonstrate working knowledge and proficiency with Microsoft Office software
Write and execute protocols and SOPs
**Only those lawfully authorized to work in the designated country associated with the position will be considered.**
**Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit . Should you have any questions/concerns, via our secure .
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' .
Job ID: 489699390
Originally Posted on: 8/16/2025
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